15 Virus 3 Flashcards

1
Q

types of immunity required

A

sterile immunity
T-cell or humoral
systemic or mucosal

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2
Q

how is sterile immunity achieved

A

it is difficult to achieve

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3
Q

what is most effective in T-cell or humoral

A

both arms most effective

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4
Q

what does systemic or mucosal need

A
class of Ig required
mucosal = IgA (short lived)
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5
Q

what do the most effective vaccines induce

A

do not induce sterile immunity - rather it builds up an amnestic response

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6
Q

what is the problem with HIV and HCV

A

Problematic for hypervariable persistent viral infections

as sterile immunity not induced

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7
Q

live viral vaccines effect

A

related non-pathogenic virus that gives cross-protection

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8
Q

example of live attenuated virus

A

cow pox protects against small pox

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9
Q

live viruses

A
  • Attenuated

- Reduce pathogenicity of a virus by passage in cell culture or non-human host

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10
Q

where is pathogenic virus located

A

from a patient and grown in human cultured cells

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11
Q

what is used to infect monkey cells

A

Cultured virus is used to infect monkey cells

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12
Q

what allows a virus to grow in monkey cells

A

Virus acquires many mutations that allow it to grow well in monkey cells

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13
Q

Advantages of live vaccines

A
  • development and production straightforward
  • low cost
  • cell-mediated (and mucosal) immunity stimulated
  • can be highly immunogenic, giving long lasting protective immunity
  • fewer inoculations that other systems required
  • live microorganisms provide continual antigenic stimulation giving sufficient time for memory cell production
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14
Q

Disadvantages of live vaccines

A
  • many cause (generally mild) disease
  • reversion to virulence may occur
  • virus shedding – potentially infect others
  • potential harm to immunocompromised individuals
  • unstable – requires continuous refrigeration
  • less safe than inactivated vaccines
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15
Q

why are recombinant proteins safe

A

No infectious agent - safe

Antigenicity of prokaryotic-expressed proteins sometimes poor - yeast or insect cell expression better

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16
Q

Recombinant surface antigen disadvantages

A

> Poorly immunogenic
Requires multiple boosts
Expensive
Problem for developing countries

17
Q

Recombinant surface antigen advantages

A

> Safe

> Also protects against Hepatitis delta virus

18
Q

what does the recombinant protein - Human Papilloma Virus cause

A

genital warts associated with cancer
Squamous cell carcinoma
Malignancy in genital tract

19
Q

Inactivated (killed) viruses

A
  • Chemical treatment, safe, poor antigenicity, humoral immunity only
  • Side effects - inflammatory responses, Purified subunits overcome this
  • Mainly induced circulatory IgG
  • Continual shedding of virus from vaccines
  • Requires repeated boosting
20
Q

what is Hepatitis A vaccine like

A

Inactivated cell culture-grown virus

21
Q

rabies injections

A

Pre and post-contact vaccination by IM injection

22
Q

rabies vaccine

A

human diploid cell vaccine

23
Q

Influenza vaccine like

A

Inactivated viral vaccine “split” or purified H and N from virus in hen eggs - allergy risk (rare)

24
Q

what does influenza protect against

A

Protects against 2 ‘Flu A strains plus 2 ‘Flu B

25
Enhancing immunogenicity
Adjuvants improve immune response potency
26
what are immunogenicity incorporated in
several human vaccines in the form of particulate aluminium salts, such as Al(OH)3 and AlPO4
27
examples of licensed adujvants
MF59 AS03 Virosomes AS04
28
MF59
Oil in water adjuvant effect in the influenza vaccine, but not when used with HSV-2 Glycoprotein
29
AS03
contains α-tocopherol, squalene and polysorbate 80 in an oil-in-water emulsion, used in pandemic influenza vaccine
30
Virosomes
Phospholipids that reconstitute influenza virosomes, used in the hepatitis A vaccine
31
AS04
Monophosphoryl lipid A (MPL) and aluminium hydroxide, approved for use in HBV (Fendrix) and HPV (Cervarix) vaccines
32
Safety concerns
Pandemic influenza vaccine associated with sudden onset narcolepsy in children
33
DNA vaccines
Inject DNA containing antigenic coding region plus promoters | - Site of injection, Persistance, Presentation pathway, Safety
34
Live vector vaccines
Use of a non-pathogenic virus or bacterium to elicit an immune response to target virus
35
how are live vector vaccines produced
genetic modification to express foreign viral genes